BEUDAMED
    FDA Adverse Event Death Summary report: N

    EUFLEXXA 20MG/2ML (6=3 SYR)

    MDR report key: 17001773 · Received May 24, 2023

    Report

    Report Number
    MW5117809
    Event Type
    Death
    Date Received
    May 24, 2023
    Date of Event
    December 16, 2022
    Report Date
    May 22, 2023
    Manufacturer
    FERRING PHARMACEUTICALS, INC.
    Product Code
    MOZ
    UDI-DI
    55566410001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE PT'S DAUGHTER REPORTS THE PT PASSED AWAY ON (B)(6) 2022. INJECT 1 SYRINGE INTO BILATERAL KNEES ONCE A WEEK FOR 3 WEEKS. PRESCRIBER INFO: (B)(6). REF REPORTS: MW5117808, MW5117810.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1618185 EUFLEXXA 20MG/2ML (6=3 SYR) ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS, INC. U10185A 55566410001

    Patients

    Seq Age Sex Outcome Treatment
    1 89 YR Female Death